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1 benefits and toxicity outcomes also favored pegylated-liposomal doxorubicin.
2 ohort of patients who were then treated with pegylated-liposomal doxorubicin.
3 oup) received doxorubicin, epirubicin or non-pegylated liposomal-doxorubicin (10 mg/kg) and cardiac f
4 herapy were treated for six 3-week cycles of pegylated liposomal doxorubicin (20 mg/m(2)) plus interl
5 -KS were randomly assigned to receive either pegylated-liposomal doxorubicin (20 mg/m2) or the combin
7 lenalidomide 25 mg, bortezomib 1.3 mg/m(2), pegylated liposomal doxorubicin 30 mg/m(2), and dexameth
8 T) and 2 lines of conventional chemotherapy (pegylated liposomal doxorubicin and docetaxel) was treat
9 luated combination lenalidomide, bortezomib, pegylated liposomal doxorubicin, and dexamethasone (RVDD
10 evidence for reduced cardiac toxicity of non-pegylated-liposomal doxorubicin characterized by attenua
11 ge (n = 102) received 4 cycles of bortezomib-pegylated liposomal doxorubicin-dexamethasone, tandem me
14 studied standard agents with rituximab plus pegylated liposomal doxorubicin (DR-COP) in an attempt t
15 e; these drugs include topotecan, etoposide, pegylated liposomal doxorubicin, epirubicin, gemcitabine
17 etermine the clinical efficacy and safety of pegylated liposomal doxorubicin in combination with gemc
22 Among 133 patients randomized to receive pegylated-liposomal doxorubicin, one achieved a complete
23 pegol versus one of the approved drugs (eg, pegylated liposomal doxorubicin or topotecan) in platinu
25 II trial evaluated vintafolide combined with pegylated liposomal doxorubicin (PLD) compared with PLD
27 icacy and safety of patupilone with those of pegylated liposomal doxorubicin (PLD) in patients with p
28 red anticancer agents 4-hydroxytamoxifen and pegylated liposomal doxorubicin (PLD) in the prevention
29 parative efficacy and safety of olaparib and pegylated liposomal doxorubicin (PLD) in this patient po
31 the efficacy and safety of a combination of pegylated liposomal doxorubicin (PLD) plus bortezomib wi
32 a multicenter phase III study that compared pegylated liposomal doxorubicin (PLD) to the BV combinat
34 the efficacy and safety of trabectedin plus pegylated liposomal doxorubicin (PLD) with that of PLD a
35 el, phase II trial evaluated the bortezomib, pegylated liposomal doxorubicin (PLD), and dexamethasone
37 After investigators selected chemotherapy (pegylated liposomal doxorubicin, weekly paclitaxel, or t
38 acy and toxicities of a new form of therapy, pegylated-liposomal doxorubicin, with standard combinati
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